EP0531568A1 - Light polarizing films and process for preparing them - Google Patents
Light polarizing films and process for preparing themInfo
- Publication number
- EP0531568A1 EP0531568A1 EP91115428A EP91115428A EP0531568A1 EP 0531568 A1 EP0531568 A1 EP 0531568A1 EP 91115428 A EP91115428 A EP 91115428A EP 91115428 A EP91115428 A EP 91115428A EP 0531568 A1 EP0531568 A1 EP 0531568A1
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- European Patent Office
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- films according
- weight
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- layers
- casting
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J5/00—Manufacture of articles or shaped materials containing macromolecular substances
- C08J5/18—Manufacture of films or sheets
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C39/00—Shaping by casting, i.e. introducing the moulding material into a mould or between confining surfaces without significant moulding pressure; Apparatus therefor
- B29C39/02—Shaping by casting, i.e. introducing the moulding material into a mould or between confining surfaces without significant moulding pressure; Apparatus therefor for making articles of definite length, i.e. discrete articles
- B29C39/12—Making multilayered or multicoloured articles
- B29C39/123—Making multilayered articles
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C41/00—Shaping by coating a mould, core or other substrate, i.e. by depositing material and stripping-off the shaped article; Apparatus therefor
- B29C41/24—Shaping by coating a mould, core or other substrate, i.e. by depositing material and stripping-off the shaped article; Apparatus therefor for making articles of indefinite length
- B29C41/28—Shaping by coating a mould, core or other substrate, i.e. by depositing material and stripping-off the shaped article; Apparatus therefor for making articles of indefinite length by depositing flowable material on an endless belt
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C41/00—Shaping by coating a mould, core or other substrate, i.e. by depositing material and stripping-off the shaped article; Apparatus therefor
- B29C41/24—Shaping by coating a mould, core or other substrate, i.e. by depositing material and stripping-off the shaped article; Apparatus therefor for making articles of indefinite length
- B29C41/32—Making multilayered or multicoloured articles
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C55/00—Shaping by stretching, e.g. drawing through a die; Apparatus therefor
- B29C55/02—Shaping by stretching, e.g. drawing through a die; Apparatus therefor of plates or sheets
- B29C55/023—Shaping by stretching, e.g. drawing through a die; Apparatus therefor of plates or sheets using multilayered plates or sheets
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/0008—Organic ingredients according to more than one of the "one dot" groups of C08K5/01 - C08K5/59
- C08K5/0041—Optical brightening agents, organic pigments
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- G—PHYSICS
- G02—OPTICS
- G02B—OPTICAL ELEMENTS, SYSTEMS OR APPARATUS
- G02B1/00—Optical elements characterised by the material of which they are made; Optical coatings for optical elements
- G02B1/08—Optical elements characterised by the material of which they are made; Optical coatings for optical elements made of polarising materials
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29K—INDEXING SCHEME ASSOCIATED WITH SUBCLASSES B29B, B29C OR B29D, RELATING TO MOULDING MATERIALS OR TO MATERIALS FOR MOULDS, REINFORCEMENTS, FILLERS OR PREFORMED PARTS, e.g. INSERTS
- B29K2029/00—Use of polyvinylalcohols, polyvinylethers, polyvinylaldehydes, polyvinylketones or polyvinylketals or derivatives thereof as moulding material
- B29K2029/04—PVOH, i.e. polyvinyl alcohol
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29K—INDEXING SCHEME ASSOCIATED WITH SUBCLASSES B29B, B29C OR B29D, RELATING TO MOULDING MATERIALS OR TO MATERIALS FOR MOULDS, REINFORCEMENTS, FILLERS OR PREFORMED PARTS, e.g. INSERTS
- B29K2995/00—Properties of moulding materials, reinforcements, fillers, preformed parts or moulds
- B29K2995/0018—Properties of moulding materials, reinforcements, fillers, preformed parts or moulds having particular optical properties, e.g. fluorescent or phosphorescent
- B29K2995/002—Coloured
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2329/00—Characterised by the use of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an alcohol, ether, aldehydo, ketonic, acetal, or ketal radical; Hydrolysed polymers of esters of unsaturated alcohols with saturated carboxylic acids; Derivatives of such polymer
- C08J2329/02—Homopolymers or copolymers of unsaturated alcohols
- C08J2329/04—Polyvinyl alcohol; Partially hydrolysed homopolymers or copolymers of esters of unsaturated alcohols with saturated carboxylic acids
Definitions
- the present invention relates to light-polarizing films containing polyvinyl alcohol and dichroic coloring components, optionally other coloring components, optionally additives and optionally surface-active compounds, characterized in that they are built up in two or more layers, at least two layers differing in their composition, and a process for their manufacture.
- PVAL polyvinyl alcohol
- iodine-containing polarizers have found technical use, which are used, for example, in passive liquid crystal displays to make the information visible.
- these films mark an excellent one Lightfastness and excellent dichroic properties in the long-wave range of the visible spectrum.
- the effective agent of these films is the iodine-PVAL complex [MM Zwick, J. Appl. Polym. Sci .; 9 2393-2424 (1965)], which, although broadband, does not completely absorb daylight.
- the short-wave (orange-yellow) range of the spectrum there is a range of reduced extinction, which is why the foils show a blue intrinsic color.
- PCR Perceived Contrast Ratio
- the iodine molecule bound in the complex has a high molar extinction, it is about 43,000 (RR Baldwin, RS Baer, RE Rundle, J.Am. Chem. Soc., 66 111 (1944)). Since the chromophore is diatomic, very high molar concentrations and thus extreme extinctions are achieved. Dyes that have a comparable molar absorption generally have significantly higher - usually 4-8 times higher - molecular weights, which is why it is difficult to obtain the required extinctions with one dye. One is forced to use very high concentrations of dyes, quickly reaching the limit of solubility in the carrier material and obtaining supersaturation effects. These can manifest themselves, for example, in undesired scattering of the light.
- At least one color triple is necessary to produce a uniform shade of gray.
- chromophores that are compatible with one another in principle in such triples, which, given the large number of properties to be achieved, means a further considerable limitation of the possibilities if the interactions cannot be harmonized. Since this is rarely completely successful, there is always the problem of overloading the matrix with dyes, which disrupts the structure of the film and leads to precipitation, instability and a decrease in dichroism.
- Another difficulty is the energy transfer, as is more frequently observed with dye mixtures, especially with anthraquinone and azo dye mixtures (Claussen, Brockes, Kops, Kröck, Neeff, Proc. SID, 26, 17-22 (1985). Because of this Resistance to light is a general difficulty of dichroic chromophores and is usually forced to be improved by using light stabilizers. These additives must be compatible with the matrix, which poses another optimization problem.
- the present invention relates to light-polarizing cast films containing polyvinyl alcohol (PVAL) and dichroic coloring components, optionally other coloring components, optionally additives and optional additives, characterized in that they are built up in two or more layers, with at least two layers in their composition differentiate.
- PVAL polyvinyl alcohol
- the at least two layers preferably differ in the type and / or the concentration of their coloring components.
- a sudden change in the composition preferably occurs.
- Casting solutions for the production of the films according to the invention are aqueous solutions of polyvinyl alcohol and coloring components (hereinafter called dyes), which may also contain additives. Solutions with a solids content of 4 to 12% by weight and a related dye content of 0.1 to 7% by weight are particularly preferred, with fluorescent dyes having a content of 0.1 and 2% by weight and others brightly colored dyes a 4-7 wt .-% based on 100 wt .-% solids content is preferred.
- dyes polyvinyl alcohol and coloring components
- the casting solutions can also contain surface-active compounds, especially anionic or amphoteric surfactants, which can be used alone or in mixtures to ensure the wetting properties of the solutions.
- the proportion of the surface-active compounds is from 0.001 to 1% by weight, preferably from 0.005 to 0.1% by weight, based on 100% by weight of casting solution.
- Suitable surface-active compounds are, for example, sulfonic acids, such as alkanesulfonic acids, in particular octyl sulfosuccinate.
- Perfluoroalkanesulfonic acids in particular perfluorooctanesulfonic acid, and their tetraalkylammonium salts, for example the tetraethylammonium salt, sulfates, in particular sulfated alkylphenol polyglycol ethers or alkylsulfonates, amphoteric surfactants, in particular alkanamidopropylbetaines, for example lauramidopropylbetaine or those in the "Chemical Abstracts" with the following REG.
- additives can also be added to the casting solutions which have a concentration-proportional effect on the dichroism and thus reinforce the dichroism of the dyes in the matrix.
- Suitable additives in the sense of the invention are e.g. lower mono- or polyhydric alcohols such as methanol, ethanol or glycol, glycerol, trimethylolethane, trimethylolpropane, pentaerythritol, sorbitol, their ethers such as glycol monomethyl ether, glycol monomethyl ether, glycol dimethyl ether, diglycol dimethyl ether, lower hydroxyamines such as propanolamine or amides such as DMF or N-pyrrolidone pyrrolidone .
- the additives can be used alone or more advantageously in mixtures, the components of the mixture also including low monohydric alcohols, e.g. Methanol, ethanol, i-propanol can occur.
- the concentration of the dichroism-enhancing additive depends on the individual properties of the dichroic dyes used. Their height is limited by the technical properties of the casting solution and the film.
- the additives are preferably added to the casting solution in amounts which make up 5-50% by weight, based on the casting solution.
- Preferred polyvinyl alcohols according to the invention are polyvinyl alcohols which have been prepared by complete or partial saponification of polyvinyl acetate, in particular types which have a viscosity> 4 mPasec, preferably 35-70 mPasec, at 20 ° C. and a degree of saponification> 80 mol in 4% aqueous solution -%, preferably 85-100 mol%.
- the invention also relates to a process for producing the polarizing films according to the invention, characterized in that the casting solutions mentioned are applied and dried two or more times on a base in a manner known per se by means of a multiple coaster, the dried film is removed from the base and then monoaxially stretched.
- All organic dyes soluble in the casting solution are suitable as dyes.
- One advantage of the process is that the component solutions can be individually optimized. It is even possible to combine incompatible dyes in the film in a mixture, for example by interposing a separating layer of undyed material between the layers in order to prevent any diffusion into the differently colored layer.
- the wet application of the layers is freely adjustable between 10 and 500 ⁇ m and can be changed to shade the structure of the film.
- a wet application of 20-250 ⁇ m is preferred, when using a curtain caster of 25-600 ⁇ m.
- Preferred dyes are those as described in DE-A 39 21 669, DE-A 3 843 414, DE-A 3 615 765 each in claim 1.
- the number of layers is greater than or equal to two, from 2 to 9 layers are preferred.
- the same dye can optionally be applied in several layers in succession.
- sequence of layers in the foils or films according to the invention can be built up sequentially or simultaneously using a cascade caster or a curtain caster.
- the light-polarizing films or foils can be compounded or laminated with other birefringence-free materials in a manner known per se.
- Suitable protective covers are e.g. Films made from a tetrafluoroethylene-hexafluoroethylene copolymer or another fluorocarbon resin, a polyester, polyolefin or polyamide resin, a polycarbonate or cellulose ester, preferably - (tri) acetate, propionate or butylate.
- a layer structure is preferred in which the light stabilizers are located in the outer protective layer.
- the layers After drying, the layers can be easily removed from the surface and stretched.
- the stretching is carried out at temperatures from 60 to 180 ° C., preferably from 100 up to 150 ° C by an amount of 300 to 1000%.
- the dye-containing films can also be post-treated, e.g. with aqueous boric acid solution to improve moisture resistance or light transmission.
- aqueous boric acid solution to improve moisture resistance or light transmission.
- the conditions under which this aftertreatment is carried out can vary regardless of the film material and dye. It is preferable to work with a 1-15% by weight, particularly preferably 5-10% by weight boric acid solution of 30-80 ° C, particularly preferably at 50-80 ° C.
- surfactants and optionally inorganic salts are added to the boric acid solution.
- the surfactants can be non-ionic, cationic or anionic; they are preferably non-ionic.
- non-ionic surfactants are: addition products of ethylene oxide with higher alcohols or phenols, for example nonylphenol. Based on water, preference is given to using 0.005-0.5% by weight, particularly preferably 0.02-0.2% by weight, of surfactant.
- Suitable inorganic salts are preferably Na sulfate, and furthermore K sulfate, Na chloride, KCl, Na nitrate, K nitrate. Based on water, 0.1-5% by weight, particularly preferably 0.3-3% by weight, of inorganic salts are preferably used. If desired, a fixation treatment can also be carried out with an aqueous solution of a high molecular weight cationic compound.
- the invention further relates to the use of the polarizing films according to the invention for the production of polarizing films.
- the polarization films that can be produced from the films according to the invention are used as polarization filters and optical displays.
- the mixture is clarified using a Seitz filter and 50 g of a 4% strength by weight aqueous solution of an anionic surfactant are added.
- the viscosity of the casting solution is now 27.3 mPas at 40 ° C.
- This solution is poured wet in a thickness of 130 ⁇ m onto a plastic belt moving at 75 m / min, over which warm air is passed in countercurrent. A smooth 11 ⁇ m thick film is obtained.
- the film is then poured with a layer thickness of 150 ⁇ m from a solution of 196 g polyvinyl alcohol (Mowiol 28-99), 40 g glycerol, 3969 g water and 6 g 4,4'-azo- (4-sulfo-azobenzene) flavonic acid (solution B) .
- a clear, ruby-colored film with a thickness of 14 ⁇ m is obtained, which after stretching 1: 6 shows a contrast ratio CR in the range from 400 to 600 nm of> 20.
- the contrast ratio CR is defined according to A. Bloom, EB Priestley, IEEE, ED 24, page 1823 (1977).
- the solutions are prepared as in Example 1 and the content of the PVAL in solution A is increased to 10% by weight. 200 ⁇ m of this solution are applied wet on a curtain coater between two 30 ⁇ m thick layers of the composition given in Example 1 in solution B and, after drying, a 25 ⁇ m thick film is obtained which, after stretching between 400 and 600 nm, has a color density of 3 and has a contrast ratio CR of 20 to 50.
- Example 1 The procedure is as in Example 1 and a two-layer film is produced. After the film has dried, a solution prepared analogously to solution A is applied to it with a wet application of 130 ⁇ m and contains Direct Blue 15 (C.I. No. 24 400) as the dye. After drying, a 21 ⁇ m thick film is obtained, which after stretching has a contrast ratio of> 20 over the visible spectral range between 400 and 650 nm, with a color density of> 2.5.
- a solution prepared analogously to solution A is applied to it with a wet application of 130 ⁇ m and contains Direct Blue 15 (C.I. No. 24 400) as the dye.
- a 21 ⁇ m thick film is obtained, which after stretching has a contrast ratio of> 20 over the visible spectral range between 400 and 650 nm, with a color density of> 2.5.
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- Polymers & Plastics (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Materials Engineering (AREA)
- Optics & Photonics (AREA)
- General Physics & Mathematics (AREA)
- Polarising Elements (AREA)
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Abstract
Description
Die vorliegende Erfindung betrifft lichtpolarisierende Filme, enthaltend Polyvinylalkohol und dichroitische farbgebende Komponenten, gegebenenfalls andere farbgebende Komponenten, gegebenenfalls Additive und gegebenenfalls oberflächenaktive Verbindungen, dadurch gekennnzeichnet, daß sie in zwei oder mehreren Schichten aufgebaut sind, wobei sich mindestens zwei Schichten in ihrer Zusammensetzung unterscheiden, sowie ein Verfahren zu ihrer Herstellung.The present invention relates to light-polarizing films containing polyvinyl alcohol and dichroic coloring components, optionally other coloring components, optionally additives and optionally surface-active compounds, characterized in that they are built up in two or more layers, at least two layers differing in their composition, and a process for their manufacture.
Filme auf der Basis von Polyvinylalkohol (PVAL), die Iod oder dichroitische Farbstoffe als polarisierende Agentien enthalten, sind bekannt.Films based on polyvinyl alcohol (PVAL) which contain iodine or dichroic dyes as polarizing agents are known.
Technische Verwendung haben bislang allein die Iod-haltigen Polarisatoren gefunden, die beispielsweise in den passiven Flüssigkristall-Displays zur Sichtbarmachung der Information eingesetzt werden. Bei Anwesenheit von Feuchtigkeit kennzeichnen diese Filme eine ausgezeichnete Lichtechtheit und hervorragende dichroitische Eigenschaften im langwelligen Bereich des sichtbaren Spektrums. Das wirksame Agens dieser Filme ist der Iod-PVAL-Komplex [M.M. Zwick, J. Appl. Polym. Sci.; 9 2393-2424 (1965)], der das Tageslicht zwar breitbandig, aber nicht vollständig absorbiert. Im kurzwelligen (orange-gelben) Bereich des Spektrums liegt ein Bereich verminderter Extinktion, weswegen die Folien eine blaue Eigenfarbe zeigen.So far, only the iodine-containing polarizers have found technical use, which are used, for example, in passive liquid crystal displays to make the information visible. In the presence of moisture, these films mark an excellent one Lightfastness and excellent dichroic properties in the long-wave range of the visible spectrum. The effective agent of these films is the iodine-PVAL complex [MM Zwick, J. Appl. Polym. Sci .; 9 2393-2424 (1965)], which, although broadband, does not completely absorb daylight. In the short-wave (orange-yellow) range of the spectrum there is a range of reduced extinction, which is why the foils show a blue intrinsic color.
Dies hat nachteilige Folgen, wenn man z.B. nach dem Durchgang durch die Folie weißes Licht erhalten will. Das unpolarisiert durchgelassene Licht vermindert den Dichroismus und damit die Polarisationsleistung in diesem Bereich. Zur Steigerung des Dichroismus ist man gezwungen, die Konzentration an Jod-Komplex zu erhöhen. Diese Korrektur im kurzwelligen Bereich zieht aber eine übermäßige Extinktion im langwelligen Bereich nach sich. Die Folge ist eine deutliche Schwächung des durchgelassenen Lichts in der Durchgangsstellung. Eine optische Anzeige, die mit dieser Folie bestückt wird, ist in ihrer Helligkeit vermindert. Um zu vertretbaren Helligkeiten zu gelangen, muß man Kompromisse schließen.This has disadvantageous consequences if e.g. wants to receive white light after passing through the film. The unpolarized transmitted light reduces the dichroism and thus the polarization performance in this area. In order to increase dichroism, one is forced to increase the concentration of iodine complex. However, this correction in the short-wave range entails excessive extinction in the long-wave range. The result is a significant weakening of the transmitted light in the through position. The brightness of an optical display that is equipped with this film is reduced. In order to achieve reasonable brightness levels, compromises have to be made.
Eine wichtige kritische Meßgröße einer universal verwendbaren optischen Anzeige ist die Ablesbarkeit bei verschiedenen Beleuchtungsverhältnissen, sie wird üblicherweise als "Perceived contrast ratio" (PCR) angegeben. Aus diesem folgt, daß die Transmission einerseits in der Sperrstellung so klein wie möglich (Ablesbarkeit bei Dunkelheit), andererseits in der Durchgangsstellung so groß wie möglich (Ablesbarkeit bei Helligkeit) gemacht werden muß. Dies erfordert eine ganz gleichmäßige, möglichst hohe Polarisationsleistung des Filters über den gesamten Bereich des sichtbaren Spektrums, welche mit der Jodfolie prinzipiell nicht erreicht werden kann.An important critical measurand of a universally usable optical display is the readability under different lighting conditions, it is usually indicated as "Perceived Contrast Ratio" (PCR). From this it follows that the transmission is as small as possible on the one hand in the blocking position (readability in the dark) and on the other hand in the through position must be made as large as possible (readability with brightness). This requires a very uniform, as high as possible polarization power of the filter over the entire range of the visible spectrum, which in principle cannot be achieved with the iodine foil.
Es hat nicht an Versuchen gefehlt, Jod durch Mischungen anderer dichroitischer Chromophore zu ersetzen, um ein Neutralgrau mit gleichmäßigen Dichroismus zu erzeugen. Allerdings bedarf es hierzu beispielsweise einer Gamme sehr leistungsfähiger Farbstoffe. Sie müssen neben guten Licht- und Wetterechtheiten eine hohe Extinktion und einen hohen Dichroismus in der Matrix aufweisen.There has been no shortage of attempts to replace iodine with mixtures of other dichroic chromophores in order to produce a neutral gray with uniform dichroism. However, this requires, for example, a range of very powerful dyes. In addition to good light and weather fastness, they must have a high extinction and a high dichroism in the matrix.
So sind vorzugsweise Polyazofarbstoffe vorgeschlagen worden (Nippon Kayaku JA 59-145 255, 60-156 759, 60-168 743). Obgleich aber der Dichroismus bei den Farbstoffen eine verbreitete Eigenschaft ist, (vgl. W. Hanle, H. Scherer, Zeitschr. Naturforsch. 6a 437-439 (1951)) gelang es bisher nicht, die spektralen Eigenschaften der Jodfolie zu erreichen oder zu übertreffen. Dies ist dem Fehlen guter Blaunuancen, der Forderung nach dem hohen Dichroismus des Systems Farbstoff/Matrix und der verlangten extremen Farbdichte im absorbierenden Zustand zuzuschreiben. Im Vergleich zu den Farbstoffen hat nämlich das im Komplex gebundene Iod-Molekül eine hohe molare Extinktion, sie beträgt etwa 43 000 (R.R. Baldwin, R.S. Baer, R.E. Rundle, J.Am. Chem.Soc., 66 111 (1944)). Da das Chromophor zweiatomig ist, erreicht man sehr hohe molare Konzentrationen und damit extreme Extinktionen. Farbstoffe, die eine vergleichbare molare Absorption haben, weisen in der Regel deutlich höhere - meist 4-8 fach höhere - Molgewichte auf, weswegen es schwer fällt, mit einem Farbstoff die verlangten Extinktionen zu erhalten. Man ist nämlich gezwungen, sehr hohe Konzentrationen an Farbstoffen einzusetzen, wobei man schnell die Grenze der Löslichkeit im Trägermaterial erreicht und Übersättigungseffekte erhält. Diese können sich beispielsweise in unerwünschten Streuungen des Lichts äußern.Polyazo dyes have preferably been proposed (Nippon Kayaku JA 59-145 255, 60-156 759, 60-168 743). However, although dichroism is a common property in dyes (cf. W. Hanle, H. Scherer, Zeitschrift. Naturforsch. 6a 437-439 (1951)), it has so far not been possible to achieve or exceed the spectral properties of iodine foil . This is due to the lack of good shades of blue, the demand for the high dichroism of the dye / matrix system and the extreme color density required in the absorbent state. Compared to the dyes, the iodine molecule bound in the complex has a high molar extinction, it is about 43,000 (RR Baldwin, RS Baer, RE Rundle, J.Am. Chem. Soc., 66 111 (1944)). Since the chromophore is diatomic, very high molar concentrations and thus extreme extinctions are achieved. Dyes that have a comparable molar absorption generally have significantly higher - usually 4-8 times higher - molecular weights, which is why it is difficult to obtain the required extinctions with one dye. One is forced to use very high concentrations of dyes, quickly reaching the limit of solubility in the carrier material and obtaining supersaturation effects. These can manifest themselves, for example, in undesired scattering of the light.
Hinzu kommt, daß zur Erzeugung eines einheitlichen Grautons mindestens ein Farbtripel notwendig ist. Natürlich kann man in solche Tripel prinzipiell nur miteinander verträgliche Chromophore einsetzen, was angesichts der Vielzahl zu leistender Eigenschaften eine weitere erhebliche Einschränkung der Möglichkeiten bedeutet, wenn es nicht gelingt, die Wechselwirkungen zu harmonisieren. Da dies selten vollkommen gelingt, hat man immer das Problem einer Überlastung der Matrix mit Farbstoffen, was den Aufbau der Folie stört und zu Ausfällungen, Instabilitäten und Senkung des Dichroismus führt.In addition, at least one color triple is necessary to produce a uniform shade of gray. Of course, one can only use chromophores that are compatible with one another in principle in such triples, which, given the large number of properties to be achieved, means a further considerable limitation of the possibilities if the interactions cannot be harmonized. Since this is rarely completely successful, there is always the problem of overloading the matrix with dyes, which disrupts the structure of the film and leads to precipitation, instability and a decrease in dichroism.
Eine weitere Schwierigkeit besteht in der Energieübertragung, wie sie bei Farbstoffmischungen, insbesondere bei Anthrachinon- und Azofarbstoff-Mischungen, häufiger beobachtet wird (Claussen, Brockes, Kops, Kröck, Neeff, Proc. SID, 26, 17-22 (1985). Deswegen ist die Beständigkeit gegen Licht eine generelle Schwierigkeit dichroitischer Chromophore. Man ist in der Regel gezwungen, sie durch Verwendung von Lichtschutzmitteln zu verbessern. Diese Additive müssen mit der Matrix verträglich sein, was ein weiteres Problem der Optimierung aufwirft.Another difficulty is the energy transfer, as is more frequently observed with dye mixtures, especially with anthraquinone and azo dye mixtures (Claussen, Brockes, Kops, Kröck, Neeff, Proc. SID, 26, 17-22 (1985). Because of this Resistance to light is a general difficulty of dichroic chromophores and is usually forced to be improved by using light stabilizers. These additives must be compatible with the matrix, which poses another optimization problem.
Die Vielfalt der Stoffe und Eigenschaften hat es bisher verhindert, eine Polarisationsfolie bereitstellen zu können, deren farbgebende Komponente nicht Iod oder ein Iod-Komplex ist, obgleich diese deutliche Vorteile in der breitbandigen Polarisationsleistung sowie der Beständigkeit gegen Feuchtigkeit und Wärme hätte.The variety of substances and properties has hitherto prevented the provision of a polarizing film whose coloring component is not iodine or an iodine complex, although this would have clear advantages in the broadband polarization performance and the resistance to moisture and heat.
Wir haben gefunden, daß man polarisierende Filme mit extrem hohen Extinktionen und störungsfreiem Aufbau dadurch erzeugen kann, daß man die Filme in zwei oder mehreren Schichten getrennt aufbaut.We have found that polarizing films with extremely high extinctions and trouble-free construction can be produced by building the films in two or more layers separately.
Gegenstand der vorliegenden Erfindung sind lichtpolarisierende Gießfolien, enthaltend Polyvinylalkohol (PVAL) und dichroitische farbgebende Komponenten, gegebenenfalls andere farbgebende Komponenten, gegebenenfalls Additive und gegebenenfalls Zusatzstoffe, gekennzeichnet dadurch, daß sie in zwei oder mehreren Schichten aufgebaut sind, wobei sich mindestens zwei Schichten in ihrer Zusammensetzung unterscheiden.The present invention relates to light-polarizing cast films containing polyvinyl alcohol (PVAL) and dichroic coloring components, optionally other coloring components, optionally additives and optional additives, characterized in that they are built up in two or more layers, with at least two layers in their composition differentiate.
Vorzugsweise unterscheiden sich die mindestens zwei Schichten in der Art und/oder der Konzentration ihrer farbgebenden Komponenten.The at least two layers preferably differ in the type and / or the concentration of their coloring components.
An der Phasengrenze der mindestens zwei sich unterscheidenden Schichten tritt vorzugsweise eine sprunghafte Änderung der Zusammensetzung auf.At the phase boundary of the at least two different layers, a sudden change in the composition preferably occurs.
Als Gießlösungen zur Herstellung der erfindungsgemäßen Folien kommen wäßrige Lösungen von Polyvinylalkohol und farbgebenden Komponenten (im folgenden Farbstoffe genannt) in Frage, die noch Additive enthalten können. Besonders bevorzugt sind Lösungen mit einem Feststoffgehalt von 4 bis 12 Gew.-% und einem darauf bezogenen Farbstoffgehalt von 0,1 bis 7 Gew.-%, wobei bei fluoreszenzfähigen Farbstoffen ein Gehalt von 0,1 und 2 Gew.-%, bei anderen bunten Farbstoffen einer von 4-7 Gew.-% bezogen auf 100 Gew.-% Feststoffgehalt bevorzugt ist.Casting solutions for the production of the films according to the invention are aqueous solutions of polyvinyl alcohol and coloring components (hereinafter called dyes), which may also contain additives. Solutions with a solids content of 4 to 12% by weight and a related dye content of 0.1 to 7% by weight are particularly preferred, with fluorescent dyes having a content of 0.1 and 2% by weight and others brightly colored dyes a 4-7 wt .-% based on 100 wt .-% solids content is preferred.
Gegebenenfalls können die Gießlösungen noch oberflächenaktive Verbindungen, besonders anionische oder amphotere Tenside enthalten, die allein oder in Mischungen eingesetzt werden können um die Benetzungseigenschaften der Lösungen zu gewährleisten. Der Anteil der oberflächenaktiven Verbindungen beträgt von 0,001 bis 1 Gew.-%, vorzugsweise von 0,005 bis 0,1 Gew.-%, bezogen auf 100 Gew.-% Gießlösung.If appropriate, the casting solutions can also contain surface-active compounds, especially anionic or amphoteric surfactants, which can be used alone or in mixtures to ensure the wetting properties of the solutions. The proportion of the surface-active compounds is from 0.001 to 1% by weight, preferably from 0.005 to 0.1% by weight, based on 100% by weight of casting solution.
Geeignete oberflächenaktive Verbindungen sind beispielsweise Sulfonsäuren, wie Alkansulfonsäuren, insbesondere Sulfobernsteinsäure-octylester. Perfluoralkansulfonsäuren, insbesondere Perfluoroctansulfonsäure, und ihre Tetraalkylammoniumsalze, beispielsweise das Tetraethylammoniumsalz, Sulfate, insbesondere sulfatierte Alkylphenolpolyglykolether oder Alkylsulfonate, amphotere Tenside, insbesondere Alkanamidopropylbetaine, beispielsweise Lauramidopropylbetain oder die in den "Chemical Abstracts" mit den folgenden REG-Nrn. aufgeführten Verbindungen:
73772-45-9, 96565-37-6, 4292-10-8, 59272-84-3, 25729-05-9, 6179-44-8, 21244-99-5, 58793-79-6, 32954-43-1, 92836-76-5 oder nichtionische Tenside wie 4-Octylphenolpolyglykolether.Suitable surface-active compounds are, for example, sulfonic acids, such as alkanesulfonic acids, in particular octyl sulfosuccinate. Perfluoroalkanesulfonic acids, in particular perfluorooctanesulfonic acid, and their tetraalkylammonium salts, for example the tetraethylammonium salt, sulfates, in particular sulfated alkylphenol polyglycol ethers or alkylsulfonates, amphoteric surfactants, in particular alkanamidopropylbetaines, for example lauramidopropylbetaine or those in the "Chemical Abstracts" with the following REG. listed connections:
73772-45-9, 96565-37-6, 4292-10-8, 59272-84-3, 25729-05-9, 6179-44-8, 21244-99-5, 58793-79-6, 32954- 43-1, 92836-76-5 or nonionic surfactants such as 4-octylphenol polyglycol ether.
Gegebenenfalls können den Gießlösungen noch Additive zugesetzt werden, die eine konzentrationsproportionale Wirkung auf den Dichroismus haben und somit den Dichroismus der Farbstoffe in der Matrix verstärken. Geeignete Additive im Sinne der Erfindung sind z.B. niedere einoder mehrwertige Alkohole wie Methanol, Ethanol oder Glykol, Glyzerin, Trimethylolethan, Trimethylolpropan, Pentaerythrit, Sorbit, deren Ether wie Glykolmonomethylether, Glykolmonomethylether, Glykoldimethylether, Diglykoldimethylether, niedere Hydroxyamine wie Propanolamin oder Amide wie DMF, N-Methylpyrrolidon, Pyrrolidon oder ε-Caprolactam. Die Additive können allein oder vorteilhafter in Mischungen eingesetzt werden, wobei als Mischungsbestandteile auch niedrige einwertige Alkohole, z.B. Methanol, Ethanol, i-Propanol auftreten können.If necessary, additives can also be added to the casting solutions which have a concentration-proportional effect on the dichroism and thus reinforce the dichroism of the dyes in the matrix. Suitable additives in the sense of the invention are e.g. lower mono- or polyhydric alcohols such as methanol, ethanol or glycol, glycerol, trimethylolethane, trimethylolpropane, pentaerythritol, sorbitol, their ethers such as glycol monomethyl ether, glycol monomethyl ether, glycol dimethyl ether, diglycol dimethyl ether, lower hydroxyamines such as propanolamine or amides such as DMF or N-pyrrolidone pyrrolidone . The additives can be used alone or more advantageously in mixtures, the components of the mixture also including low monohydric alcohols, e.g. Methanol, ethanol, i-propanol can occur.
Die Konzentration des Dichroismus-verstärkenden Additivs ist von der individuellen Eigenschaften der eingesetzten dichroitischen Farbstoffe abhängig. Ihre Höhe ist durch die technischen Eigenschaften der Gießlösung und der Folie beschränkt.The concentration of the dichroism-enhancing additive depends on the individual properties of the dichroic dyes used. Their height is limited by the technical properties of the casting solution and the film.
Die Additive werden der Gießlösung vorzugsweise in Mengen zugesetzt, die 5-50 Gew.-%, bezogen auf die Gießlösung ausmachen.The additives are preferably added to the casting solution in amounts which make up 5-50% by weight, based on the casting solution.
Bevorzugte erfindungsgemäße Polyvinylalkohole sind Polyvinylalkohole, die durch vollständige oder teilweise Verseifung von Polyvinylacetat hergestellt worden sind, insbesondere Typen, die in 4 %iger wäßriger Lösung eine Viskosität > 4 mPasec, vorzugsweise 35-70 mPasec, bei 20°C und einen Verseifungsgrad > 80 Mol-%, vorzugsweise 85-100 Mol-% aufweisen.Preferred polyvinyl alcohols according to the invention are polyvinyl alcohols which have been prepared by complete or partial saponification of polyvinyl acetate, in particular types which have a viscosity> 4 mPasec, preferably 35-70 mPasec, at 20 ° C. and a degree of saponification> 80 mol in 4% aqueous solution -%, preferably 85-100 mol%.
Gegenstand der Erfindung ist auch ein Verfahren zur Herstellung der erfindungsgemäßen polarisierenden Filme, dadurch gekennzeichnet, daß man die genannten Gießlösungen in an sich bekannter Weise zwei oder mehrmals auf einer Unterlage mittels eines Mehrfachgießers anträgt und trocknet, den getrockneten Film von der Unterlage löst und anschließend monoaxial verstreckt.The invention also relates to a process for producing the polarizing films according to the invention, characterized in that the casting solutions mentioned are applied and dried two or more times on a base in a manner known per se by means of a multiple coaster, the dried film is removed from the base and then monoaxially stretched.
Als Farbstoffe kommen alle in der Gießlösung löslichen organischen Farbstoffe in Frage. Ein Vorteil des Verfahrens ist es, die Lösungen der Bestandteile einzeln optimieren zu können. Man kann sogar in einer Mischung unverträgliche Farbstoffe in der Folie kombinieren, indem man beispielsweise eine Trennschicht aus ungefärbtem Material zwischen die Schichten zwischengießt, um eine eventuelle Diffusion in die jeweils anders gefärbte Schicht zu verhindern.All organic dyes soluble in the casting solution are suitable as dyes. One advantage of the process is that the component solutions can be individually optimized. It is even possible to combine incompatible dyes in the film in a mixture, for example by interposing a separating layer of undyed material between the layers in order to prevent any diffusion into the differently colored layer.
Der Naßauftrag der Schichten ist zwischen 10 und 500 µm frei einstellbar und kann zur Nuancierung des Aufbaus der Folie verändert werden. Bei Einsatz eines Kaskadengießers zur Herstellung der Schichten ist ein Naßauftrag von 20 - 250µm, bei Verwendung eines Vorhanggießers von 25 - 600 µm bevorzugt.The wet application of the layers is freely adjustable between 10 and 500 µm and can be changed to shade the structure of the film. When using a cascade caster for the production of the layers, a wet application of 20-250 µm is preferred, when using a curtain caster of 25-600 µm.
Bevorzugte Farbstoffe sind solche, wie sie in DE-A 39 21 669, DE-A 3 843 414, DE-A 3 615 765 jeweils in Anspruch 1 beschrieben sind.Preferred dyes are those as described in DE-A 39 21 669, DE-A 3 843 414, DE-A 3 615 765 each in claim 1.
Die Anzahl der Schichten ist größer oder gleich zwei, bevorzugt sind von 2 bis 9 Schichten. Zu Erhöhung der Farbdichte kann der gleiche Farbstoff gegebenenfalls in mehreren Schichten hintereinander aufgezogen werden.The number of layers is greater than or equal to two, from 2 to 9 layers are preferred. To increase the color density, the same dye can optionally be applied in several layers in succession.
Die Schichtenfolge in den erfindungsgemäßen Folien oder Filmen kann zeitlich nacheinander oder gleichzeitig unter Verwendung eines Kaskadengießers oder eines Vorhanggießers aufgebaut werden.The sequence of layers in the foils or films according to the invention can be built up sequentially or simultaneously using a cascade caster or a curtain caster.
Die lichtpolarisierenden Filme oder Folien können in an sich bekannter Weise mit anderen doppelbrechungsfreien Materialien compoundiert oder laminiert werden. Als Schutzüberzug eignen sich z.B. Folien aus einem Tetrafluorethylen-hexafluorethylen-Copolymer oder einem anderen Fluorkohlenwasserstoff-Harz, einem Polyester-, Polyolefin- oder Polyamid-Harz, einem Polycarbonat oder Celluloseester, vorzugsweise -(tri)acetat, -propionat oder -butylrat.The light-polarizing films or foils can be compounded or laminated with other birefringence-free materials in a manner known per se. Suitable protective covers are e.g. Films made from a tetrafluoroethylene-hexafluoroethylene copolymer or another fluorocarbon resin, a polyester, polyolefin or polyamide resin, a polycarbonate or cellulose ester, preferably - (tri) acetate, propionate or butylate.
Bevorzugt ist ein Schichtaufbau, bei dem die Lichtstabilisatoren in der äußeren Schutzschicht liegen.A layer structure is preferred in which the light stabilizers are located in the outer protective layer.
Die Schichten lassen sich nach dem Trocknen leicht von der Unterlage lösen und recken. Das Verstrecken erfolgt bei Temperaturen von 60 bis 180°C vorzugsweise von 100 bis 150°C um einen Betrag von 300 bis 1000 %. Nach Verkleben mit einer optisch isotropen und im sichtbaren Spektralgebiet leeren Folie erhält man Polarisationsfolien mit einem sehr guten dichroitischen Verhältnis und einer frei wählbaren Nuance.After drying, the layers can be easily removed from the surface and stretched. The stretching is carried out at temperatures from 60 to 180 ° C., preferably from 100 up to 150 ° C by an amount of 300 to 1000%. After gluing with an optically isotropic film that is empty in the visible spectral region, polarizing films with a very good dichroic ratio and a freely selectable shade are obtained.
Gewünschtenfalls können die farbstoffhaltigen Filme auch einer Nachbehandlung, z.B. mit wäßriger Borsäurelösung, zwecks Verbesserung der Feuchtebeständigkeit oder der Lichtdurchlässigkeit unterworfen werden. Die Bedingungen, unter denen diese Nachbehandlung durchgeführt wird, können unabhängig vom Filmmaterial und Farbstoff schwanken. Vorzugsweise arbeitet man mit einer 1-15 gew.-%igen, besonders bevorzugt 5-10 gew.-%igen Borsäurelösung von 30-80°C, besonders bevorzugt bei 50-80°C. Vorzugsweise setzt man der Borsäurelösung Tenside und gegebenenfalls anorganische Salze zu. Die Tenside können nicht-ionisch, kationisch oder anionisch sein, bevorzugt sind sie nicht-ionisch.If desired, the dye-containing films can also be post-treated, e.g. with aqueous boric acid solution to improve moisture resistance or light transmission. The conditions under which this aftertreatment is carried out can vary regardless of the film material and dye. It is preferable to work with a 1-15% by weight, particularly preferably 5-10% by weight boric acid solution of 30-80 ° C, particularly preferably at 50-80 ° C. Preferably, surfactants and optionally inorganic salts are added to the boric acid solution. The surfactants can be non-ionic, cationic or anionic; they are preferably non-ionic.
Beispiele für nicht-ionische Tenside sind: Additionsprodukte von Ethylenoxid an höhere Alkohole oder Phenole, beispielsweise Nonylphenol. Vorzugsweise verwendet man, bezogen auf Wasser, 0,005-0,5 Gew.-%, besonders bevorzugt 0,02-0,2 Gew`-% Tensid. Als anorganische Salze kommen vorzugsweise Na-sulfat, und weiterhin K-sulfat, Na-chlorid, KCl, Na-nitrat, K-nitrat in Betracht. Bezogen auf Wasser werden vorzugsweise 0,1-5 Gew.-%, besonders bevorzugt 0,3-3 Gew.-% anorganische Salze eingesetzt. Gewünschtenfalls kann noch eine Fixierungsbehandlung mit einer wäßrigen Lösung einer hochmolekularen kationischen Verbindung vorgenommen werden.Examples of non-ionic surfactants are: addition products of ethylene oxide with higher alcohols or phenols, for example nonylphenol. Based on water, preference is given to using 0.005-0.5% by weight, particularly preferably 0.02-0.2% by weight, of surfactant. Suitable inorganic salts are preferably Na sulfate, and furthermore K sulfate, Na chloride, KCl, Na nitrate, K nitrate. Based on water, 0.1-5% by weight, particularly preferably 0.3-3% by weight, of inorganic salts are preferably used. If desired, a fixation treatment can also be carried out with an aqueous solution of a high molecular weight cationic compound.
Gegenstand der Erfindung ist ferner die Verwendung der erfindungsgemäßen polarisierenden Filme zur Herstellung von Polarisationsfolien.The invention further relates to the use of the polarizing films according to the invention for the production of polarizing films.
Die aus den erfindungsgemäßen Filmen herstellbaren Polarisationsfolien finden als Polarisationsfilter und optische Anzeigen Verwendung.The polarization films that can be produced from the films according to the invention are used as polarization filters and optical displays.
Einer Mischung aus 224 g Polyvinylalkohol (Mowiol 28-99 Viskosität nach DIN 53 015:28 ± 2 mPas, Hydrolysegrad 99,4 ± 0,4 Mol-%, Esterzahl 8 ± 5 mg KOH/g, Hersteller Hoechst AG), 4552 g Wasser, 45 g Glycerin und 372 g Methanol werden 7 g 4,4'-Azo-[3-(2-sulfo-4-hydroxi-6-N-benzoylamino-)naphthalin]-stilben-2-sulfonsäure hinzugefügt und unter Rühren gelöst (Lösung A). Nach 12 h Rührzeit bei einer Temperatur von 90°C wird über ein Seitz-Filter geklärt und 50 g einer 4 gew.-%igen wäßrigen Lösung eines anionischen Tensids hinzugegeben. Die Viskosität der Gießlösung beträgt jetzt 27,3 mPas bei 40°C.A mixture of 224 g of polyvinyl alcohol (Mowiol 28-99 viscosity according to DIN 53 015: 28 ± 2 mPas, degree of hydrolysis 99.4 ± 0.4 mol%, ester number 8 ± 5 mg KOH / g, manufacturer Hoechst AG), 4552 g Water, 45 g of glycerol and 372 g of methanol are added to 7 g of 4,4'-azo- [3- (2-sulfo-4-hydroxy-6-N-benzoylamino-) naphthalene] -stilbene-2-sulfonic acid and with stirring solved (solution A). After a stirring time of 12 hours at a temperature of 90 ° C., the mixture is clarified using a Seitz filter and 50 g of a 4% strength by weight aqueous solution of an anionic surfactant are added. The viscosity of the casting solution is now 27.3 mPas at 40 ° C.
Diese Lösung wird in 130 µm Dicke naß auf ein mit 75 m/min bewegtes Kunststoffband gegossen, über das Warmluft im Gegenstrom geführt wird. Man erhält einen glatten 11 µ dicken Film.This solution is poured wet in a thickness of 130 µm onto a plastic belt moving at 75 m / min, over which warm air is passed in countercurrent. A smooth 11 μm thick film is obtained.
Anschließend übergießt man den Film mit 150 µm Schichtdicke einer Lösung aus 196 g Polyvinylalkohol (Mowiol 28-99), 40 g Glycerin, 3969 g Wasser und 6 g 4,4'Azo-(4-sulfo-azobenzol)flavonsäure (Lösung B). Man erhält einen in der Durchsicht tief rubinfarbenen Film der Dicke 14 µm, der nach dem Recken 1:6 ein Kontrastverhältnis CR im Bereich von 400 bis 600 nm von >20 zeigt. Das Kontrastverhältnis CR ist entsprechend A. Bloom, E.B. Priestley, IEEE, ED 24, Seite 1823 (1977) definiert.The film is then poured with a layer thickness of 150 μm from a solution of 196 g polyvinyl alcohol (Mowiol 28-99), 40 g glycerol, 3969 g water and 6 g 4,4'-azo- (4-sulfo-azobenzene) flavonic acid (solution B) . A clear, ruby-colored film with a thickness of 14 μm is obtained, which after stretching 1: 6 shows a contrast ratio CR in the range from 400 to 600 nm of> 20. The contrast ratio CR is defined according to A. Bloom, EB Priestley, IEEE, ED 24, page 1823 (1977).
Zur Herstellung der Lösungen verfährt man wie in Beispiel 1 und erhöht den Gehalt des PVAL in Lösung A auf 10 Gew.-%. Man trägt 200 µm dieser Lösung zwischen zwei 30 µm dicken Schichten der in Beispiel 1 in Lösung B gegebenen Zusammensetzung auf einem Vorhanggießer naß an und erhält nach dem Trocknen einen 25 µm dicken Film, der nach dem Recken zwischen 400 und 600 nm eine Farbdichte von 3 und ein Kontrastverhältnis CR von 20 bis 50 hat.The solutions are prepared as in Example 1 and the content of the PVAL in solution A is increased to 10% by weight. 200 μm of this solution are applied wet on a curtain coater between two 30 μm thick layers of the composition given in Example 1 in solution B and, after drying, a 25 μm thick film is obtained which, after stretching between 400 and 600 nm, has a color density of 3 and has a contrast ratio CR of 20 to 50.
Man verfährt wie in Beispiel 1 und erzeugt einen zweischichtigen Film. Nach dem Trocknen des Films trägt man auf diesen eine analog Lösung A hergestellte Lösung mit einem Naßauftrag von 130 µm an, die als Farbstoff Direct Blue 15 (C.I. Nr. 24 400) enthält. Nach dem Trocknen erhält man einen in der Aufsicht schwarzen 21 µm dicken Film, der nach dem Recken ein Kontrastverhältnis von >20 über den sichtbaren Spektralbereich zwischen 400 und 650 nm hat, bei einer Farbdichte von >2,5.The procedure is as in Example 1 and a two-layer film is produced. After the film has dried, a solution prepared analogously to solution A is applied to it with a wet application of 130 μm and contains Direct Blue 15 (C.I. No. 24 400) as the dye. After drying, a 21 µm thick film is obtained, which after stretching has a contrast ratio of> 20 over the visible spectral range between 400 and 650 nm, with a color density of> 2.5.
Claims (10)
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DE19904026892 DE4026892A1 (en) | 1990-08-25 | 1990-08-25 | LIGHT-POLARIZING FILMS AND A METHOD FOR THEIR PRODUCTION |
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Cited By (7)
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EP1367085A2 (en) * | 2002-05-20 | 2003-12-03 | Eastman Kodak Company | Polyvinyl alcohol films prepared by coating methods |
EP1367083A2 (en) * | 2002-05-20 | 2003-12-03 | Eastman Kodak Company | Optical films prepared by coating methods |
US7012746B2 (en) | 2002-05-20 | 2006-03-14 | Eastman Kodak Company | Polyvinyl butyral films prepared by coating methods |
US7048823B2 (en) | 2002-05-20 | 2006-05-23 | Eastman Kodak Company | Acrylic films prepared by coating methods |
US7125504B2 (en) | 2002-11-13 | 2006-10-24 | Eastman Kodak Company | Optical switch microfilms |
US7393579B2 (en) | 2002-05-20 | 2008-07-01 | Eastman Kodak Company | Cellulose acetate films prepared by coating methods |
US7686987B2 (en) | 2002-05-20 | 2010-03-30 | Eastman Kodak Company | Polycarbonate films prepared by coating methods |
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JP4573404B2 (en) * | 2000-07-18 | 2010-11-04 | 株式会社クラレ | Manufacturing method of polarizing film |
JP4693978B2 (en) * | 2000-11-09 | 2011-06-01 | 株式会社クラレ | Polyvinyl alcohol film and method for producing the same |
JP4485045B2 (en) * | 2000-11-15 | 2010-06-16 | 株式会社クラレ | Method for producing vinyl alcohol polymer film for drawing |
JP4060174B2 (en) * | 2001-12-17 | 2008-03-12 | 株式会社クラレ | Polyvinyl alcohol film and polarizing film |
DE102005031966B4 (en) * | 2005-07-08 | 2011-10-27 | Günter Grau | Production of a polarization-sensitive filter with targeted expansion and orientation for CCD or CMOS image sensors |
JP4805117B2 (en) * | 2006-12-13 | 2011-11-02 | 株式会社クラレ | Manufacturing method of polarizing film |
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GB2144760A (en) * | 1983-08-04 | 1985-03-13 | Photophysics Research Limited | Light-polarising material |
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JPS5614533A (en) * | 1979-07-16 | 1981-02-12 | Shin Etsu Chem Co Ltd | Production of polarizing film or sheet |
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1990
- 1990-08-25 DE DE19904026892 patent/DE4026892A1/en not_active Withdrawn
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1991
- 1991-08-21 JP JP3232476A patent/JPH04271302A/en active Pending
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GB2144760A (en) * | 1983-08-04 | 1985-03-13 | Photophysics Research Limited | Light-polarising material |
Cited By (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP1367085A2 (en) * | 2002-05-20 | 2003-12-03 | Eastman Kodak Company | Polyvinyl alcohol films prepared by coating methods |
EP1367083A2 (en) * | 2002-05-20 | 2003-12-03 | Eastman Kodak Company | Optical films prepared by coating methods |
EP1367085A3 (en) * | 2002-05-20 | 2004-12-08 | Eastman Kodak Company | Polyvinyl alcohol films prepared by coating methods |
EP1367083A3 (en) * | 2002-05-20 | 2004-12-15 | Eastman Kodak Company | Optical films prepared by coating methods |
US7012746B2 (en) | 2002-05-20 | 2006-03-14 | Eastman Kodak Company | Polyvinyl butyral films prepared by coating methods |
US7048823B2 (en) | 2002-05-20 | 2006-05-23 | Eastman Kodak Company | Acrylic films prepared by coating methods |
US7163738B2 (en) | 2002-05-20 | 2007-01-16 | Eastman Kodak Company | Polyvinyl alcohol films prepared by coating methods |
US7393579B2 (en) | 2002-05-20 | 2008-07-01 | Eastman Kodak Company | Cellulose acetate films prepared by coating methods |
US7686987B2 (en) | 2002-05-20 | 2010-03-30 | Eastman Kodak Company | Polycarbonate films prepared by coating methods |
US7125504B2 (en) | 2002-11-13 | 2006-10-24 | Eastman Kodak Company | Optical switch microfilms |
Also Published As
Publication number | Publication date |
---|---|
DE4026892A1 (en) | 1992-02-27 |
JPH04271302A (en) | 1992-09-28 |
EP0531568B1 (en) | 1997-03-12 |
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